LOCATOR Angled Abutment
K-Number: K243272 · 2025-01-14
ApplicantZest Anchors, LLC
Decision Date2025-01-14
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
LOCATOR Angled Abutment is a medical device manufactured by Zest Anchors, LLC. It received FDA 510(k) clearance on 2025-01-14 under approval number K243272. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LOCATOR Angled Abutment?
LOCATOR Angled Abutment is a medical device that received FDA 510(k) clearance on 2025-01-14. It is manufactured by Zest Anchors, LLC. The 510(k) number is K243272.
When was LOCATOR Angled Abutment approved by the FDA?
LOCATOR Angled Abutment received FDA 510(k) clearance on 2025-01-14, under approval number K243272.
What company makes LOCATOR Angled Abutment?
LOCATOR Angled Abutment is manufactured by Zest Anchors, LLC.
What is the FDA product code for LOCATOR Angled Abutment?
The FDA product code for LOCATOR Angled Abutment is NHA.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.